Maruyama Hitoshi, Takahashi Masanori, Shimada Taro, Yokosuka Osamu
Department of Medicine and Clinical Oncology, Chiba University Graduate School of Medicine, Chiba, Japan.
Scand J Gastroenterol. 2012 Jun;47(6):686-91. doi: 10.3109/00365521.2012.674972. Epub 2012 Apr 4.
To determine the safety and efficacy of anticoagulation treatment for portal vein thrombosis in cirrhosis patients with acute variceal bleeding, with patient eligibility determined by contrast ultrasonography findings.
This prospective study included 23 consecutive cirrhosis patients (63.8 ± 11.8 years old, 12 males and 11 females) with emergency admission for acute variceal bleeding with or without portal vein thrombus. Eligibility for anticoagulation treatment was determined by positive intra-thrombus enhancement on contrast ultrasonography (perflubutane microbubble agent, 0.0075 mL/kg) performed before endoscopy. Low-molecular-weight heparin was administered after hemostasis was achieved by band ligation. Repeated band ligation or injection sclerotherapy combined with argon plasma coagulation was performed for variceal disappearance.
Hemostasis was achieved in all 10 patients with active bleeding. Five of these patients had portal vein thrombus, and all showed positive intra-thrombus enhancement on contrast ultrasonography. Anticoagulation treatment of these five patients resulted in complete recanalization of the portal vein within 2-11 days. There were no significant differences in the number of endoscopic treatment sessions or the length of hospital stay between the groups with and without thrombosis, and no complications including rebleeding were reported. Long term, none of the patients who continued oral anticoagulation treatment had recurrence of thrombosis (4/5). Variceal recurrence occurred only in the non-thrombosis group (2/18) during the follow-up period (median: 351 days).
Early anticoagulation treatment in cirrhosis patients with portal vein thrombosis and acute variceal bleeding may be safe, tolerated, and effective in cases with positive intra-thrombus enhancement on contrast ultrasonography.
通过对比超声检查结果确定患者入选标准,以判定抗凝治疗对肝硬化合并急性静脉曲张出血患者门静脉血栓形成的安全性和有效性。
本前瞻性研究纳入了23例连续的肝硬化患者(年龄63.8±11.8岁,男性12例,女性11例),这些患者因急性静脉曲张出血伴或不伴门静脉血栓而急诊入院。在内镜检查前通过对比超声(全氟丁烷微泡剂,0.0075 mL/kg)检查血栓内增强情况来确定是否适合进行抗凝治疗。在通过套扎术实现止血后给予低分子量肝素。对于静脉曲张消失,采用重复套扎术或注射硬化疗法联合氩离子凝固术。
所有10例活动性出血患者均实现了止血。其中5例患者存在门静脉血栓,且在对比超声检查中均显示血栓内增强阳性。对这5例患者进行抗凝治疗后,门静脉在2至11天内完全再通。有血栓形成组和无血栓形成组在内镜治疗次数或住院时间方面无显著差异,且未报告包括再出血在内的并发症。长期来看,继续口服抗凝治疗的患者中无一例发生血栓复发(4/5)。在随访期(中位时间:351天)内,仅非血栓形成组发生了静脉曲张复发(2/18)。
对于门静脉血栓形成且合并急性静脉曲张出血的肝硬化患者,在对比超声检查显示血栓内增强阳性的情况下,早期抗凝治疗可能是安全、可耐受且有效的。